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American Journal of Human Genetics|November 9, 2010
To identify associations with rare variants, just WHaIT: Weighted haplotype and imputation-based testsYun Li, Andrea E Byrnes, Mingyao LiAmerican Journal of Human Genetics|November 9, 2010
Mutations in myosin light chain kinase cause familial aortic dissectionsLi Wang, Dong-chuan Guo, Jiumei Cao, et al.American Journal of Human Genetics|August 10, 2010
Whole-genome genetic diversity in a sample of Australians with deep Aboriginal ancestryBrian P McEvoy, Joanne M Lind, Eric T Wang, et al.American Journal of Human Genetics|August 10, 2010
Microdeletions of 3q29 confer high risk for schizophreniaJennifer Gladys Mulle, Anne F Dodd, John A McGrath, et al.American Journal of Human Genetics|April 9, 2011
Insights into the pathogenesis and treatment of cancer from inborn errors of metabolismAyelet Erez, Oleg A Shchelochkov, Sharon E Plon, et al.American Journal of Human Genetics|April 9, 2011
Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic researchMichael E Talkowski, Carl Ernst, Adrian Heilbut, et al.American Journal of Human Genetics|February 1, 1990
GM2-gangliosidosis B1 variant: analysis of beta-hexosaminidase alpha gene abnormalities in seven patientsA Tanaka, K Ohno, K Sandhoff, et al.American Journal of Human Genetics|August 1, 1990
Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotypeJ R Korenberg, H Kawashima, S M Pulst, et al.American Journal of Human Genetics|September 1, 1987
Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22)J M Trent, I L Flink, E Morkin, et al.American Journal of Human Genetics|November 5, 1997
D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorderY Suzuki, L L Jiang, M Souri, et al.Pageof 979